NA10995
DNA from Fibroblast
Description:
TRANSLOCATED CHROMOSOME
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Chromosome Abnormalities dbGaP |
Quantity |
10 µg |
Quantitation Method |
Please see our FAQ |
Cell Type
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Fibroblast
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Transformant
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Untransformed
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Sample Source
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DNA from Fibroblast
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Race
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White
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Family Member
|
1
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Relation to Proband
|
proband
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Confirmation
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Karyotypic analysis after cell line submission to CCR
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ISCN
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46,XY,der(11)t(1;11)(q31;q25)pat.arr 1q31.3q44(192686117-247190999)x3,11q25(133290323-134449982)x1
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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Passage Frozen |
5 |
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IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis |
|
Cytogenetics |
Chromosome 1: DERIVATIVE CHROMOSOME Aneuploid Segment (+)1q31>1qter |
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Chromosome 1: DERIVATIVE CHROMOSOME Trisomic Segment 1q31>1qter |
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Chromosome 11: DERIVATIVE CHROMOSOME Aneuploid Segment (-)11q25>11qter |
Remarks |
Expired 45 minutes post delivery with multicystic dysplasia of kidneys, IUGR, atrial septal defect, persistent left superior vena cava and malpositioned hair whorl; sister and father, GM10958 and GM10960 Lymph, have the balanced translocation |
Treff NR, Zimmerman R, Bechor E, Hsu J, Rana B, Jensen J, Li J, Samoilenko A, Mowrey W, Van Alstine J, Leondires M, Miller K, Paganetti E, Lello L, Avery S, Hsu S, Melchior Tellier LCA, Validation of concurrent preimplantation genetic testing for polygenic and monogenic disorders, structural rearrangements, and whole and segmental chromosome aneuploidy with a single universal platform European journal of medical genetics62:103647 2019 |
PubMed ID: 31026593 |
|
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
PubMed ID: 23665875 |
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